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CD161(+)和不变自然杀伤 T 细胞参与儿童哮喘恶化。

Participation of CD161(+) and invariant natural killer T cells in pediatric asthma exacerbations.

机构信息

Departamento de Investigaciones Inmunológicas, Instituto de Diagnóstico y Referencia Epidemiológicos, Mexico City, Mexico.

出版信息

Allergy Asthma Proc. 2013 Jan-Feb;34(1):84-92. doi: 10.2500/aap.2013.34.3619.

Abstract

Asthma has been defined as a disease of chronic airway inflammation in which many cells and cellular products participate with variable degrees of airflow obstruction and hyperresponsiveness that lead to recurrent episodes of wheezing, breathlessness, chest tightness, and coughing. Prominent among these cellular elements are two cell types referred to as the invariant natural killer T (iNKT) cells and a subpopulation of T cells expressing the molecule CD161, which are both thought to play a role in the pathogenesis of asthma. Although the presence of iNKT and other CD161(+) cells in murine models has been associated with asthma, relatively few studies have been performed in the adult patient with asthma that have been often conflicting and even fewer studies are available in children. The present study was performed to investigate the peripheral blood frequencies of iNKT and CD161(+) T cells in children with asthma. A total of 35 children, 19 stable asthmatic patients, 6 who had experienced an asthmatic attack within 24 hours and had not received any treatment, and 10 healthy controls, aged 6-12 years, were enrolled in the study. iNKT and CD161(+) T-cell frequencies in blood were measured together with quantitative levels of IL-4 and interferon (IFN) γ using a cytofluorimetric approach. The results show that iNKT cells are increased in pediatric asthmatic patients undergoing exacerbations of asthma. These cells also produced less IFN-γ and more IL-4 than children with stable asthma and in healthy control children. These results suggest that iNKT cells might participate in the development of the asthmatic exacerbations. The increased production of IL-4 in conjunction with the decrease of IFN-γ may be mechanistically responsible, at least partially, for the heightening of the immunologic response leading to the asthmatic attack in children. Knowledge of these interactive mechanisms involving the iNKT cell and our understanding of its role in the exacerbation of asthma hold great promise in the development of better diagnostic predictive markers of disease progression as well as new forms of therapeutic interventions.

摘要

哮喘被定义为一种慢性气道炎症性疾病,其中许多细胞和细胞产物参与其中,其气流阻塞和高反应性的程度不同,导致反复出现喘息、呼吸困难、胸闷和咳嗽。在这些细胞成分中,两种细胞类型被认为在哮喘发病机制中起作用,它们分别是称为不变自然杀伤 T(iNKT)细胞和表达分子 CD161 的 T 细胞亚群。虽然在小鼠模型中存在 iNKT 和其他 CD161(+)细胞与哮喘有关,但在哮喘成年患者中进行的研究相对较少,而且往往相互矛盾,在儿童中可用的研究更少。本研究旨在调查哮喘儿童外周血 iNKT 和 CD161(+)T 细胞的频率。共纳入 35 名儿童,其中 19 名稳定哮喘患者、6 名在 24 小时内发生哮喘发作且未接受任何治疗的患者和 10 名健康对照者,年龄 6-12 岁。使用流式细胞仪法测量血液中 iNKT 和 CD161(+)T 细胞的频率,并同时测量 IL-4 和干扰素(IFN)γ 的定量水平。结果表明,在哮喘发作的儿科哮喘患者中,iNKT 细胞增加。这些细胞产生的 IFN-γ 少于稳定哮喘患儿和健康对照儿童,而产生的 IL-4 多于稳定哮喘患儿和健康对照儿童。这些结果表明,iNKT 细胞可能参与了哮喘加重的发展。IL-4 产生增加与 IFN-γ 减少相结合,可能至少部分地负责导致儿童哮喘发作的免疫反应增强的机制。了解这些涉及 iNKT 细胞的相互作用机制及其在哮喘加重中的作用,为开发更好的疾病进展预测标志物以及新的治疗干预形式提供了很大的希望。

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